An organic electroluminescent element includes an optically transparent electrode, a counter electrode, an emission layer, an auxiliary reflective layer and a diffusion-preventing layer. The counter electrode is paired with the optically transparent electrode and formed of ag or an alloy containing ag and has light reflectivity. The emission layer is disposed between the optically transparent electrode and the counter electrode. The auxiliary reflective layer is disposed on an opposite side of the counter electrode from the emission layer. The diffusion-preventing layer is disposed between the counter electrode and the auxiliary reflective layer whose components are prevented from diffusing and moving therebetween.
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1. An organic electroluminescent element comprising:
an optically transparent electrode;
a counter electrode which is paired with the optically transparent electrode and formed of ag or an alloy containing ag and has light reflectivity;
an emission layer disposed between the optically transparent electrode and the counter electrode;
an auxiliary reflective layer disposed on an opposite side of the counter electrode from the emission layer; and
a diffusion-preventing layer which is disposed between the counter electrode and the auxiliary reflective layer whose components are prevented from diffusing and moving therebetween, the diffusion-preventing layer having insulation properties.
2. The organic electroluminescent element according to
the counter electrode has a refractive index of 0.17 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm,
the counter electrode has an extinction coefficient of 5.0 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm.
3. The organic electroluminescent element according to
the diffusion-preventing layer has an extinction coefficient of 0.1 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm.
4. The organic electroluminescent element according to
the diffusion-preventing layer is thinner than the counter electrode.
5. The organic electroluminescent element according to
the diffusion-preventing layer contains a material of which dipole moment is 0.1 D or more.
6. The organic electroluminescent element according to
the auxiliary reflective layer is electrically conductive, and
the auxiliary reflective layer is electrically connected to the counter electrode in a region where the emission layer is not formed.
7. The organic electroluminescent element according to
an optically transparent substrate disposed on an opposite side of the optically transparent electrode from the emission layer; and
a light out-coupling structure disposed on a surface, on a side of the optically transparent electrode, of the optically transparent substrate.
8. A lighting device comprising:
the organic electroluminescent element according to
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An invention relating to organic electroluminescent elements and lighting devices including the same is disclosed.
An organic electroluminescent element has been known in general, which is hereinafter also referred to as an “organic EL element”. The organic EL element has a structure in which functional layers like a hole injection layer, a hole transport layer, an emission layer, an electron transport layer, and an electron injection layer are stacked between a cathode and an anode disposed on a substrate. In the organic EL element, voltage is applied between the anode and the cathode, where by planate light is emitted outward from the emission layer.
In the organic EL element, light is emitted outward through an optically transparent electrode. There has been known a light out-coupling structure where an electrode paired with the optically transparent electrode is composed of a reflective electrode so that light from the emission layer is reflected by the reflective electrode to be emitted outward. By using the reflective electrode, it is possible to efficiently emit the light outward.
In the organic EL element, light out-coupling efficiency is important, and a structure to improve light out-coupling property more has been developed. In Japanese Patent Publication Number 2003-123987, a technique for obtaining a high brightness is disclosed, in which an emission layer is disposed between a total reflection mirror and a half mirror, thereby forming a resonant structure. However, in this structure, it is difficult to adjust a thickness of each layer, and it may be hard to form the organic EL element.
Further, as the structure for improving light reflectivity, it is conceivable to increase reflective index of the reflective electrode. For example, the reflectivity of the electrode can be expected to be improved by using silver as an electrode material because silver is a metal having high reflectivity.
It is not however easy to improve electrical reliability of the electrode containing silver because silver has property to be stacked to sneak during film formation, thereby facilitating the occurrence of short circuit when a foreign matter is mixed. Also, using a lot of silver in order to improve reflectivity can cause high-cost and decreasing of economic efficiency
The invention disclosed below is aim at providing an organic electroluminescent element and a lighting device, each of which has improved reflectivity, high out-coupling efficiency and high electrical reliability, and suppresses short circuit.
The organic EL element is disclosed. The organic EL element includes an optically transparent electrode, a counter electrode, an emission layer, an auxiliary reflective layer and a diffusion-preventing layer. The counter electrode is paired with the optically transparent electrode, and formed of Ag or an alloy containing Ag and has light reflectivity. The emission layer is disposed between the optically transparent electrode and the counter electrode. The auxiliary reflective layer is disposed on an opposite side of the counter electrode from emission layer. The diffusion-preventing layer is disposed between the counter electrode and the auxiliary reflective layer. The diffusion-preventing layer prevents components from diffusing and moving between the counter electrode and the auxiliary layer.
The lighting device is disclosed. The lighting device includes the above organic EL element and wiring.
In the above organic EL element and lighting device, the counter electrode contains silver, and the auxiliary reflective layer and the diffusion-preventing layer is disposed. Therefore, the reflectivity can be improved, the short circuit can be suppressed, and the light out-coupling efficiency and the electrical reliability can be increased.
An organic electroluminescent element (an organic EL element) according to the invention is disclosed. The organic EL element includes an optically transparent electrode 2, a counter electrode 4 which is paired with the optically transparent electrode 2 and has light reflectivity, and an emission layer 3 disposed between the optically transparent electrode 2 and the counter electrode 4. The counter electrode 4 is formed of Ag or an alloy containing Ag. An auxiliary reflective layer 6 is disposed on an opposite side of the counter electrode 4 from emission layer 3. A diffusion-preventing layer 5 is disposed between the auxiliary reflective layer 6 and the counter electrode 4. The diffusion-preventing layer 5 prevents components from diffusing and moving between the counter electrode 4 and the auxiliary reflective layer 6. In this organic EL element, the counter electrode 4 containing silver and the auxiliary reflective layer 6 being disposed, thereby improving reflectivity. Also, even in the case of the counter electrode 4 formed of silver or silver alloy, because of the counter electrode 4 having thin enough to reflect by the auxiliary reflective layer 6, it is possible to suppress a short circuit. And also, the diffusion-preventing layer 5 is disposed between the auxiliary reflective layer 6 and the the counter electrode 4, whereby it is possible to suppress reduction in reflectivity and denaturalization of the electrical property caused by diffusion of components. It is therefore possible to improve light reflectivity and the light out-coupling efficiency and electrical reliability, and prevent the short circuit.
An organic layer 9 is formed of functional layers including the emission layer 3 and disposed between the optically transparent electrode 2 and the counter electrode 4. The whole of the organic layer 9 includes a collection of the functional layers. An organic luminant 10 includes a stack of the optically transparent electrode 2, the organic layer 9 and the counter electrode 4. Further, when there is no hindrance to emit light, the organic layer 9 may be a structure formed of a single emission layer 3.
The organic luminant 10 is disposed on a surface of the optically transparent substrate 1. The optically transparent substrate 1 is a substrate which sustains a luminous stack. The organic luminant 10 is formed by stacking each layer in order on the optically transparent substrate 1. For example, in
In the organic EL element shown in
The optically transparent substrate 1 is formed of an appropriate substrate material. For example, it may be glass. With glass, the organic luminant 10 can be made and sustained well. It is also possible to suppress an invasion of the water, and deterioration of the organic layer 9. In the case of using glass, glass having high reflective index can be used. As a result, it is possible to reduce a difference in a refractive index. The refractive index of the glass having high refractive index is about 1.7 to 1.9. Of course, ordinary glass whose refractive index is 1.7 or less may be used. The optically transparent substrate 1 may be also formed of plastic. By using the optically transparent substrate 1 formed of plastic, it is possible to improve handle ability. In this case, plastic preferably has a moisture-proof. Because plastic has flexibility, it is possible to form a flexible element. Furthermore, as the optically transparent substrate 1, a composite substrate formed of a stack of a glass layer and a plastic layer can be used. In the composite substrate, it is possible to improve the light out-coupling property. In the case where the optically transparent substrate 1 is formed of the composite substrate, preferably the glass layer is disposed on a light emission side (an outside), and the plastic layer is disposed on a side of the optically transparent electrode 2 (an inside). As a result, it is possible to improve the light out-coupling property and the moisture-proof.
The optically transparent electrode 2 can be formed of an appropriate electrode material. Examples thereof include a metal thin film having optically transparency, a metal oxide film, and the like. Examples of the metal oxide film include ITO, IZO, AZO, and the like. The optically transparent electrode 2 may be also formed of a film layer of a metal oxide film and a metal thin film. Example of the film layer include ITO/Ag, Ag/ITO, Ag alloy/ITO, ITO/Ag alloy, and the like. Here, the material for the counter electrode 4 can be used as Ag alloy. Note that in the examples of the film layer “/” represents a layer boundary, a material in front of “/” represents an under layer (a side of the light transmitting substrate 1), and a material behind “/” represents an upper layer (a side of the counter electrode 4). The optically transparent electrode 2 can form an anode and a cathode. The optically transparent electrode 2 is preferably the anode.
Preferably, the optically transparent electrode 2 has a small extinction coefficient in a visible light region. For example, the optically transparent electrode 2 may have the extinction coefficient of 0.05 or less in the visible light region, but is not limited thereto.
The optically transparent electrode 2 preferably has a charge mobility of 30 cm2/Vs or more, and a carrier density of 1×1021 cm−3 or less. Therefore, when optically transparent electrodes 2 have the same resistance value, it is possible to suppress light absorption in a region close to an infrared region of the visible light region, and reduce a loss of absorption. In other words, when the charge mobility and the carrier density are out of this range, in case that they have the same resistance value, causes a tendency to increase the extinction coefficient in the near-infrared region, and light absorbency. On the other hand, by setting the charge mobility and the carrier density as mentioned above, it is possible to suppress the phenomenon. This has been confirmed by experiments. Although there is no upper limit of the charge mobility, it may be 50 cm2/Vs or less, for example. The carrier density is preferably 1×1020/cm3 or more, more preferably 5×1020/cm3 or more.
The organic layer 9 forms a functional layer cluster, which is a collection of the functional layers, between the the optically transparent electrode 2 and the counter electrode 4. The organic layer 9 forming the functional layer cluster has a stack of appropriate layers for emitting light by driving the organic EL element. At least one of functional layers is the emission layer 3. The emission layer 3 is a layer containing emitting materials. The emission layer 3 is a layer that emits light as a result of combination of electrons and holes. The emission layer 3 include dopants as emitting materials and base materials for doping the dopant in general.
The organic layer 9 may have multiple emission layers 3. In this case, respective emitting materials of emission layers 3 may be different from each other. And also, respective light wavelengths of the emitting materials may be different from each other. For example, various colors can be made by providing at least three emission layers 3 including a red emission layer, a green emission layer and a blue emission layer to emit light with three colors of red, green and blue. Especially, three colors light emission enables to emit white light and obtain an useful organic EL element for lighting. In addition, for example, white light emission can be obtained from two colors light emission of blue and orange. However, three colors light emission has better luminescence property than two colors light emission.
In the case where emission layers 3 are provided, the single emission layer 3 is shown in
The organic layer 9 may have only one emission layer 3. In this case, it is possible to obtain the organic EL element with simple structure. Multiple emitting materials may be used even in either one emission layer 3 or multiple emission layers 3. Therefore, even in the case of one emission layer 3, the emission layer 3 contains multiple emitting materials having different wavelengths, whereby white light can be emitted. However, preferably emission layers 3 are provided in order to well emit white light for lighting.
Besides the emission layer 3, examples of each functional layer forming the organic layer 9 include a hole injection layer, a hole transport layer, an electron transport layer, an electron injection layer, an intermediate layer, and the like. Layers other than the emission layer 3 in the organic layer 9 generally include a functional layer having a function to transport charges (holes or electrons). Here, layers other than the emission layer 3 of the organic layer 9 are defined as a charge transfer layer 8. The charge transfer layer 8 may have a multi-layer structure or a single layer structure. In other words, the charge transfer layer 8 may have a function to transport charges (holes or electrons).
The charge transfer layer 8 is formed of a first charge transfer layer 8a disposed on the optically transparent electrode 2 side of the emission layer 3, and a second charge transfer layer 8b disposed on the counter electrode 4 side of the emission layer 3. In the case where the optically transparent electrode 2 forms the anode and the counter electrode 4 forms the cathode, the first charge transfer layer 8a can be formed of a layer having a function to move holes. Moving holes can be defined as the hole injection and/or transport. In this case, for example, the first charge transfer layer 8a can be formed of the hole injection layer and the hole transport layer from the side of the optically transparent electrode 2. In the case where the optically transparent electrode 2 forms an anode and the counter electrode 4 forms a cathode, the second charge transfer layer 8b can be formed of a layer having a function to move electrons. Moving an electron can be defined as the electron injection and/or transporting. In this case, for example, the second charge transfer layer 8b can be formed of the electron injection layer and the electron transport layer.
Here, a layer touching the counter electrode 4, of functional layers forming the charge transfer layer 8 may be formed of a charge injection layer. In the case where the counter electrode 4 forms the cathode, the charge injection layer is the electron injection layer. The charge injection layer may be a layer of a metal simple substance whose work function is small. For example, the charge injection layer (the electron injection layer) can be formed of Li, Mg, Na, Cs, or the like. However, in the case where the charge injection layer is formed of a layer of the metal simple substance, preferably the charge injection layer has the thickness of 10 nm or less in order to improve the light out-coupling property. Especially in the embodiment, since the counter electrode 4 can be formed of a thin film, preferably the charge injection layer has the thickness in the thickness region. From the viewpoint of charge injection properties, the thickness of the charge injection layer is, for example, 1 nm or more. A mixed film of metal and an organic film can be used as the charge injection layer (the electron injection layer). The mixed film can be formed of a layer where the metal is contained in the organic layer. The thickness of the the charge injection layer in this case is not particularly limited. Examples of the mixed film serving as the electron injection layer include a mixed film of Li and the electron-transporting organic film, a mixed film of Na and the electron-transporting organic film, the mixed film of an alkali metal or an alkaline earth metal and the electron-transporting film, the mixed film of LiO2 or Liq and the electron-transporting organic film, and the like. Examples of the mixed film include a mixed film of organic electronic dopant and the electron-transporting organic film and the like. Note that the charge injection layer is a part of the charge transfer layer 8, and part of the organic layer 9. The organic layer 9 can be defined as a stacking structure in which it is disposed between the optically transparent electrode 2 and the counter electrode 4. Here, even if the charge injection layer is formed of a metal simple substance, the stacking structure is the organic layer 9 that is disposed between the optically transparent electrode 2 and the counter electrode 4. The organic layer 9 may be the stacking structure in which an organic material is contained as a whole, and include an inorganic layer as a part thereof.
The counter electrode 4 is an electrode which is electrically paired with the optically transparent electrode 2. When voltage is applied between the optically transparent electrode 2 and the counter electrode 4, a current flows therebetween and light is generated in the emission layer 3.
One of the optically transparent electrode 2 and the counter electrode 4 forms the anode, and the other forms the cathode. In one embodiment, the optically transparent electrode 2 can form the anode, and the counter electrode 4 can form the cathode. In other embodiment, the optically transparent electrode 2 can form the cathode, and the counter electrode 4 can form the anode. In the organic EL element shown in
The counter electrode 4 may be formed of Ag or an alloy containing Ag. By using Ag or an alloy containing Ag (AG-alloy), the light reflectivity can be improved. High light reflectivity can be obtained by using silver because silver has higher light reflectivity in the visible light region than other metallic materials that can be a light reflective electrode. Also, because silver has high conductivity, even if the counter electrode 4 is thinned, it is possible to ensure a function as an electrode.
The counter electrode 4 preferably has light reflectivity. Light can therefore escape from the side of the optically transparent electrode 2 by reflecting light traveling to the side of the counter electrode 4 from the emission layer 3 to change a path of light to the side of the optically transparent electrode 2. However, the counter electrode 4 preferably transmits part of light, rather than reflecting the whole of the light. In other words, the counter electrode 4 preferably has optical transparency. Therefore, because the counter electrode 4 is such a thin film so that it transmits the light, it is possible to suppress a short circuit and easily obtain light reflectivity by the auxiliary reflective layer 6. The counter electrode 4 is preferably formed as a light reflecting electrode having optical transparency.
The alloy containing Ag (Ag-alloy) contains, for example, Ag as the main component and the alloy contains at least one metal selected from Al, Pt, Rh, Mg, Au, Cu, Zn, Ti, Pd, Nd, Bi, and Ni. Especially, AgBi, AgPd, AgMg, AgNdCu, AgPdCu, or the like are exemplified. Ag-alloy is preferably high in the ratio of Ag. Therefore, it is possible to improve light reflectivity. For example, the weight ratio of Ag in the Ag alloy is preferably 90% or more, more preferably 95% or more, further more preferably 98% or more, most preferably 99% or more.
As shown in
In stacking process, the optically transparent electrode 2 can be formed as a layer whose surface is flat. As shown in
Here, on the occasion of stacking, there is a case where a foreign matter X is mixed during stacking process.
As shown in
When the counter electrode 4 is then formed, because silver which is the material of the counter electrode 4 is easy to sneak when it is formed, it can easily intrude and be stacked into the gap between the foreign matter X and the second organic layer 9b (the organic layer 9). The silver is liable to sneak in comparison with other metallic materials for light reflection electrodes.
At this time, as shown in
However, as shown in
The counter electrode 4 can be formed of a thin film. In other words, the counter electrode 4 can formed of an Ag thin film or an Ag alloy thin film. The counter electrode 4 containing Ag is a thin film, thereby being capable of suppressing sneaking of Ag to improve electrical reliability.
Preferably a thickness of the counter electrode 4 is less than 120 nm. The counter electrode 4 is formed of Ag or alloy containing Ag, but, when the thickness of the counter electrode 4 is over 120 nm, stacking Ag may be liable to cause the short circuit. When the counter electrode 4 is thick, the counter electrode 4 is close to pure silver. When the counter electrode 4 is thick, an amount of silver increases, thereby making it difficult to form the counter electrode 4. In the case where the thickness of the counter electrode 4 is over 120 nm, possibility to totally reflect light is increased, and reflex by the auxiliary reflective layer 6 is hard to be obtained. From a viewpoint thereof, the thickness of the counter electrode 4 is more preferably 110 nm or less. The thickness of the counter electrode 4 is still more preferably 60 nm or less. Therefore, it is possible to further suppress a shot circuit.
The thickness of the counter electrode 4 is preferably 10 nm or more. Therefore, it is possible to improve a light reflectivity of the counter electrode 4, and to obtain high reflex by silver or alloy containing silver. And, when the thickness of the counter electrode 4 is too thin, there is a risk that a conductivity of the counter electrode 4 decreases. However, because silver has high conductivity, when the thickness of the counter electrode 4 is less than 10 nm, it is possible to secure enough conductivity. The thickness of the counter electrode 4 is preferably in thickness region of 10 to 60 nm. The More preferable thickness of the counter electrode 4 is set by a material of the auxiliary reflective layer 6 and a thickness of that.
The counter electrode preferably has a refractive index of 0.17 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm. It is therefore possible to easily form the counter electrode 4 having light reflectivity and optical transparency. A wavelength in the range of 440 nm to 460 nm is a representative wavelength of blue. A wavelength in the range of 550 nm to 570 nm is a representative wavelength of green. A wavelength in the range of 610 nm to 630 nm is a representative wavelength of red. Therefore, when the refractive index is low in blue, green and red wavelengths, from a short wavelength to a long wavelength in a visible light region, the counter electrode 4 can have advantageous structure. Preferably the refractive index of the counter electrode 4 is 0.17 or less in a whole visible region. The counter electrode 4 can therefore have more advantageous structure. The whole visible region may be the wavelength region of 400 nm to 780 nm. The refractive index of the counter electrode 4 is preferably as low as possible, a lower limit thereof is not particularly limited, but from a viewpoint of production, the refractive index of the counter electrode 4 may be 0.01 or more. Further, the refractive index of the counter electrode 4 may be 0.05 or more.
The counter electrode 4 preferably has an extinction coefficient of 5.0 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm. It is therefore possible to suppress light absorption by the counter electrode 4, and easily form the counter electrode 4 having both light reflectivity and optically transparency. A wavelength in the range of 440 nm to 460 nm is a representative wavelength of blue. A wavelength in the range of 550 nm to 570 nm is a representative wavelength of green. A wavelength in the range of 610 nm to 630 nm is a representative wavelength of red. Therefore, when the extinction coefficient is low in blue, green and red wavelengths, from a short wavelength to a long wavelength in a visible light region, the counter electrode 4 can have a more advantageous structure. The extinction coefficient of the counter electrode 4 is preferably 5.0 or less in a whole visible light region. The counter electrode 4 can therefore have further advantageous structure. The whole visible region may be the wavelength region of 400 nm to 780 nm. The extinction coefficient of the counter electrode 4 is preferably as low as possible, a lower limit therefore is not particularly limited, but from a viewpoint of production, the extinction coefficient of the counter electrode 4 may be 0.5 or more. The extinction coefficient of the counter electrode 4 may be 1.0 or more.
The counter electrode 4 preferably has reflectivity in a visible light region. An upper limit of the reflective index of the counter electrode 4 is not limited, but from a viewpoint of suppressing the short circuit and obtaining available reflection by the auxiliary reflective layer 6, the reflective index of the counter electrode 4 in the visible light region may be 90% or less. Further, in order to prevent the short circuit, the reflective index of the counter electrode 4 in the visible region may be 50% or less.
The auxiliary reflective layer 6 is a layer supporting a reflection of the counter electrode 4. The auxiliary reflective layer 6 is disposed on an opposite side of the counter electrode 4 from emission layer 3. As described above, in the case where the counter electrode 4 is thin, part of light passes therethrough to travel to an opposite side thereof from a light out-coupling side (a side of the optically transparent electrode 2). Therefore, by disposing the auxiliary reflective layer 6, it is possible to reflect the light passing through the counter electrode 4 to turn a traveling direction of the light to the side of the optically transparent electrode 2. It is therefore possible to improve the light out-coupling property. In the organic EL element, light reflecting structure which reflects light from the emission layer 3 is formed of the counter electrode 4 having reflectivity and the auxiliary reflective layer 6.
In the auxiliary reflective layer 6, light reflectance in a visible light region is preferably 60% or more. It is therefore possible to reflect more light and improve the light-coupling property. The reflective index of the auxiliary reflective layer 6 in the visible light region is preferably 70% or more, still more preferably 80% or more, and most preferably 90% or more. Preferably the auxiliary reflective layer 6 has a high light reflectance, but an upper limit thereof is not limited, but in consideration of light absorption and material properties, light reflectance of the auxiliary reflective layer 6 may be 95% or less.
The auxiliary reflective layer 6 is preferably formed of metal materials. It is therefore possible to obtain high light reflectivity easily. Examples of metal materials used for the auxiliary reflective layer 6 include, but not limited to, Al, Mg, Ca, Ti, Cu, Au, an alloy of these and the like. Al and Mg of these materials are more preferable as the material of the auxiliary reflective layer 6. Al and Mg have relatively uniformly high reflectivity in the whole visible light region, and therefore auxiliary reflectivity can be improved. Al is preferably used in particular. Al can suppress a reduction loss in reflectivity of a thinned counter electrode 4, provide easy stacking process. Al is relatively cheap material, and can therefore provide easy production. Of cause, the auxiliary reflective layer 6 may be formed of light reflective materials except metal materials. For example, a reflective layer formed of SiO2 or TiO2 may be used. The auxiliary reflective layer 6 may exclude Ag. By excluding Ag, more easy production can be provided.
The thickness of the auxiliary reflective layer 6 is preferably 30 nm or more. It is therefore possible to improve the reflectivity of the auxiliary reflective layer 6. The thickness of the auxiliary reflective layer 6 is more preferably 50 nm or more. An upper limit of the thickness of the auxiliary reflective layer 6 is not limited in particular, but when the thickness of the auxiliary reflective layer 6 is too thick, there is a possibility of wasting materials, and generating a side effect that a deposition process time is increased. Therefore, the thickness of the auxiliary reflective layer 6 is preferably 200 nm or less. The thickness of the auxiliary reflective layer 6 is preferably thicker than that of the counter electrode 4. It is therefore possible to obtain high auxiliary reflex. More preferable thickness of the auxiliary reflective layer 6 can be set depending on the material of the auxiliary reflective layer 6, the material of the counter electrode 4, and the thickness of the counter electrode 4.
By the way, the auxiliary reflective layer 6 may be formed of Ag or an alloy containing Ag. In this case, it is possible to get high light reflectance. Also, the diffusion-preventing layer 5 is disposed between the counter electrode 4 and the auxiliary reflective layer 6. Therefore, the gap by the foreign matter X is filled by the diffusion-preventing layer 5, and silver sneaking during deposition can be suppressed, and the short circuit can be suppressed. In this case, the diffusion-preventing layer 5 serves as the layer which suppress silver sneaking (sneaking-suppressing layer). However, when the auxiliary reflective layer 6 is thin, there is a possibility that short circuit caused by the silver sneaking cannot be suppressed sufficiently. Also, when the auxiliary reflective layer 6 is formed of silver, there is a possibility that economic efficiency will go down by materials being expensive. Therefore, the auxiliary reflective layer 6 preferably excludes Ag.
The diffusion-preventing layer 5 is a layer which can prevent components from diffusing and moving between the counter electrode 4 and the auxiliary reflective layer 6. The diffusion-preventing layer 5 is disposed between the auxiliary reflective layer 6 and the counter electrode 4. The diffusion-preventing layer 5 is a barrier, and diffusing of components from the counter electrode 4 to the auxiliary reflective layer 6 and diffusing of components from the auxiliary reflective layer 6 to the counter electrode 4 are suppressed. It is therefore possible to improve reflectivity.
Here, as a structure for improving reflectivity, a structure to dispose the auxiliary reflective layer 6 so that it touches the counter electrode 4 can be exemplified. However, when the counter electrode 4 is in directly contact with the auxiliary reflective layer 6, there is a possibility that components diffuse and move by an interdiffusion between the counter electrode 4 and the auxiliary reflective layer 6. In the organic EL element, a temperature rises along with a drive in general, and an interdiffusion is likely to occur at higher temperature. For example, when the auxiliary reflective layer 6 of metal material is stacked directly on the counter electrode 4 formed of Ag or alloy containing Ag, metals in the auxiliary reflective layer 6 diffuses with time, and metals are mixed into the counter electrode 4. A phenomenon called migration can occur. Specifically, in the case where the counter electrode 4 is formed of only Ag, Ag is alloyed. In the case where the counter electrode 4 is formed of Ag alloy, other metals different from Ag alloy are mixed or a content ratio of metals varies, thereby denaturing a composition of the Ag alloy. When metals other than Ag or Ag-alloy which originally forms the counter electrode 4 are mixed into the counter electrode 4, there is a concern that reflectivity reduces. When metals other than Ag or Ag-alloy which originally forms the counter electrode 4 are also mixed into the counter electrode 4, there is a concern that electrical property of the counter electrode 4 is denatured. Accordingly, in the above organic EL element, the diffusion-preventing layer 5 is disposed between the counter electrode 4 and the auxiliary reflective layer 6. Therefore, components diffusion between the counter electrode 4 and the auxiliary reflective layer 6 are suppressed, and accordingly it is possible to suppress a temporal decrease with time in reflectance and denaturation of electrical properties. By separating the counter electrode 4 and the auxiliary reflective layer 6, moving of atoms and/or molecules is prevented, and interdiffusion is suppressed. In this embodiment, the diffusion-preventing layer 5 is disposed so that it touches the counter electrode 4, and the diffusion-preventing layer 5 is disposed so that it touches the auxiliary reflective layer 6.
The diffusion-preventing layer 5 preferably has an extinction coefficient of 0.1 or less in wavelength regions of 440 to 460 nm, 550 to 570 nm and 610 to 630 nm. It is therefore possible to suppress wastefully absorbing of light by the diffusion-preventing layer 5, and obtain higher reflectivity by the auxiliary reflective layer 6. A wavelength in the range of 440 nm to 460 nm is a representative wavelength of blue. A wavelength in the range of 550 nm to 570 nm is a representative wavelength of green. A wavelength in the range of 610 nm to 630 nm is a representative wavelength of red. Therefore, when the extinction coefficient is low in blue, green and red wavelengths from a short wavelength to a long wavelength in a light visible region, the diffusion-preventing layer 5 can have a more advantageous structure. The extinction coefficient of the diffusion-preventing layer 5 is preferably 0.01 or less in the whole visible light region. The diffusion-preventing layer 5 can further have a more advantageous structure. The whole visible light region may be a wavelength region of 400 to 780 nm. The extinction coefficient of the diffusion-preventing layer 5 may be as low as possible, and the lower limit is not limited in particular, from the viewpoint of the production, the extinction coefficient of the diffusion-preventing layer 5 may be 0.0001 or more.
The diffusion-preventing layer 5 is preferably thinner than the counter electrode 4. It is therefore possible to improve reflective efficiency and the light out-coupling property. When the thickness of the diffusion-preventing layer 5 is thicker than the thickness of the counter electrode 4, there is a concern that light absorption by the diffusion-preventing layer 5 becomes larger. When the thickness of the diffusion-preventing layer 5 is thick, a light interference effect by light passing through the counter electrode 4 becomes larger, and reflectivity as a whole light reflecting structure may decrease. Therefore, the diffusion-preventing layer 5 is preferably thinner than the counter electrode 4.
The diffusion-preventing layer 5 preferably has a thickness of 5 nm or more. It is therefore possible to improve an effect of preventing diffusion of components. The diffusion-preventing layer 5 preferably has a thickness of 20 nm or less. It is therefore possible to suppress light absorption by the diffusion-preventing layer 5 and reduce an effect of light interference. The the diffusion-preventing layer 5 more preferably has a thickness of 10 nm or less.
In a preferable embodiment, the diffusion-preventing layer 5 has insulation properties. When the diffusion-preventing layer 5 has conductive property, there is a concern that interdiffusion occurs between the diffusion-preventing layer 5 and the counter electrode 4.
The diffusion-preventing layer 5 preferably contains material of which dipole moment is 0.1 D or more. It is therefore possible to improve an effect of suppressing the diffusion of components. By using a substance having polarity by dipole moment of 0.1 D or more, an effect of suppressing the diffusion of components from the auxiliary reflective layer 6 to the counter electrode 4 and the diffusion of components from the counter electrode 4 to the auxiliary reflective layer 6 are improved. An upper limit of the dipole moment is not limited in particular, but may be, for example, 10 D or less.
The diffusion-preventing layer 5 may be formed of appropriate materials preventing interdiffusion between the counter electrode 4 and the auxiliary reflective layer 6. The diffusion-preventing layer 5 may preferably be formed of inorganic materials. Inorganic materials can suppress light absorption and improve diffusion-preventing effect by the diffusion-preventing layer 5. Of course, the diffusion-preventing layer 5 may be formed of organic materials like resins. In this case, the organic material having low reflectivity is preferably used. The diffusion-preventing layer 5 may be formed of various materials that can be used as a hole transport layer or an electron transport layer in the organic layer 9. Examples of materials of the diffusion-preventing layer 5 include NPB, BCP, TPD, Bphen, CBP and the like.
Examples of materials of the diffusion-preventing layer 5 include metal fluoride, metal oxide, silicon oxide, silicon nitride, metal nitride, silicon oxynitride, metal oxynitride, and the like. These materials may have insulation properties. Of these, materials of which dipole moment is 0.1 D or more are preferably used. Specifically, examples of materials of the diffusion-preventing layer 5 include LiF, MgF2, SiO2, AL2O3, SiON, TiON, and the like. LiF of the examples is more preferable. In the case of LiF, it is possible to obtain a high effect of preventing the diffusion and provide easy production.
The diffusion-preventing layer 5 and the auxiliary reflective layer 6 can be formed by an appropriate method. In a preferable embodiment, the diffusion-preventing layer 5 is formed by vapor deposition or spattering. It is therefore possible to efficiently form the diffusion-preventing layer 5 that is thin. In a preferable embodiment, the auxiliary reflective layer 6 is formed by vapor deposition or spattering. It is possible therefore to efficiently form the auxiliary reflective layer 6 having high reflectivity. Preferably the counter electrode 4, the diffusion-preventing layer 5 and the auxiliary reflective layer 6 are formed by the same stacking process. In this case, these layers can be continuously stacked and formed, and accordingly layers can be formed efficiently.
In the organic EL element, the organic luminant 10 is normally sealed. Moisture intrusion from the outside is suppressed by sealing, and deterioration of the element can be suppressed. In an example of
In the organic EL element of
The electrical connection of the auxiliary reflective layer 6 and the counter electrode 4 may be carried out by directly connecting the auxiliary reflective layer 6 with the counter electrode 4. It is therefore possible to easily electrically connect them. Here, when the auxiliary reflective layer 6 is directly contacted with the counter electrode 4, the interdiffusion may occur, but it is possible to reduce the influence on the light emission even if the interdiffusion occurs because part in which the auxiliary reflective layer 6 is electrically connected with the counter electrode 4 is a region which is not overlapped with the emission layer 3.
Preferably the auxiliary reflective layer 6 is electrically connected to the counter electrode 4 on the outside of the emission layer 3 in planar view. It is therefore possible to electrically connect the auxiliary reflective layer 6 and the counter electrode 4 without preventing light emission at the center of a plane of the emission layer 3. In
The diffusion-preventing layer 5 is preferably equal to or larger than the emission layer 3 in planar view. It is therefore possible to obtain a high effect of preventing the diffusion of components in a region where the emission layer 3 is formed.
When the organic EL element of
Preferably the organic EL element includes an optically transparent substrate 1 that is disposed on the opposite side of the optically transparent electrode 2 from the emission layer 3. The light out-coupling structure 11 is disposed on a surface, on a side of the optically transparent electrode 2, of the optically transparent substrate 1. Refractive index difference in a substrate interface and total reflection are reduced by disposing the light out-coupling structure 11, and therefore more light will escape. In the case where light is reflected by the auxiliary reflective layer 6 as described above, light reflected by the counter electrode 4 and light reflected by the auxiliary reflective layer 6 are mixed as reflected light, but the reflected light can escape more efficiently by forming the light out-coupling structure 11.
In
In a more preferable embodiment, the light out-coupling structure 11 includes a roughness structure 11c. The roughness structure 11c is preferably disposed in an interface of the stacking structure including the first transparent material layer 11a and the second transparent material structure 11b. In roughness structure 11c, light is scattered by roughness interface, and it is therefore possible to suppress total reflection by the surface of the optically transparent substrate 1 and improve the light out-coupling property. The roughness structure 11c may be fine irregularities of nanometer order. It is therefore provided with light scattering property, and can further improve light out-coupling property. The roughness structure 11c is preferably disposed in an interface of a low refractive index layer and a high refractive index layer. The low refractive index layer and the high refractive index layer may be formed of resins. The high refractive index layer may contain high refractive index particles in order to adjust refractive index.
As another embodiment of the light out-coupling structure 11, the light out-coupling structure 11 including resins mixed with particles that causes disturbance to light refraction can be used. In this case, the light out-coupling structure 11 may be a single layer. The light out-coupling structure 11 may also include structure where the surface of the optically transparent electrode 2 side of the optically transparent substrate 1 is roughness surface.
Preferably, in each of above embodiments, light out-coupling structure is further provided on a surface of outside of the optically transparent substrate 1 (on an opposite side thereof from the optically transparent electrode 2). This light out-coupling structure may be provided with a light out-coupling layer, or formed so that the optically transparent substrate 1 has a roughness surface. The light out-coupling structure can be formed of, for example, a light scattering structure. For example, the light out-coupling structure can be easily formed by sticking an optical film. In the case where the light out-coupling structure is provided on both side of the optically transparent substrate 1, it is possible to improve light out-coupling property.
In
In the embodiment of
The lighting device has the above organic EL element. Since the lighting device has the organic EL element, the lighting device having good luminescent can be obtained. For example, a light-emitting face of one organic EL element can be shaped like a rectangle having a width of 10 cm or more and a depth of 10 cm or more, but is not limited to this. The lighting device may have multiple organic EL elements arranged in layers. The lighting device may have wiring structure that supplies electricity to the organic EL element. The lighting device may have a housing configured to support the organic EL element. The lighting device may have plug configured to electrically connect the organic EL element and a power supply. The lighting device can be formed like a panel. The lighting device can be formed like a plane. The lighting device can be thinned, and accordingly it is possible to provide a space-saving lighting device.
In order to confirm that above reflecting structure is useful, a stack with the counter electrode, the diffusion-preventing layer and the auxiliary reflective layer (Working example 1) was formed and a stack with the counter electrode and the auxiliary reflective layer and without the diffusion-preventing layer (Comparative example 1) was formed, of which temporal reflectivity were put to the test. The counter electrode was an Ag layer having the thickness of 30 nm, the diffusion-preventing layer was a LiF layer having the thickness of 5 nm, and the auxiliary reflective layer was an Al layer having the thickness of 60 nm. Temporal reflectivity was identified by comparing the early light reflectance (0 h) and the light reflectance after heating treatment at 90 C for 71 hour (71 h). A reflective sheet formed, as a counter electrode, of Ag layer having the thickness of 120 nm (Comparative example 2), and a reflective sheet formed, as a counter electrode, of Al layer having the thickness of 100 nm (Comparative example 3) were formed for comparison, and reflective indexes thereof were identified. When Comparative example 2 was used as the counter electrode of the organic EL element, the short circuit caused by the thick Ag layer was identified.
Furthermore, an organic EL element including stacking structure (Working example 2) was formed. In the stacking structure, the light out-coupling structure is between the optically transparent substrate and the optically transparent electrode, and includes the low refractive index layer and the high refractive index layer, and has the roughness structure in an interface thereof. This organic EL element includes a counter electrode of an Ag layer having the thickness of 15 nm, a diffusion-preventing layer of a LiF layer having the thickness of 8 nm, and an auxiliary reflective layer of an Al layer having the thickness of 50 nm. The organic EL element with an Ag layer as the counter electrode having the thickness of 100 nm and without the diffusion-preventing layer, the auxiliary reflective layer and the light out-coupling structure, obtained by Comparative example 3, was formed as comparison. A test comparing electrical property of the organic EL element of Working example 2 with that of the organic EL element of Comparative example 3 was carried out. Result of electrical property is shown in TABLE. 1.
As shown in TABLE. 1, Working example 2 had higher brightness, higher electrical power efficiency, higher external quantum efficiency and higher color rendering (R9, Ra) than Comparative example 3. Particularly, it was identified that light out-coupling efficiency (external quantum efficiency) was improved by 16%.
TABLE 1
Working
Comparative
example 2
example 3
light reflecting structure
Ag(15)/LiF(8)/
Al(100)
(film thickness: nm)
AL(50)
voltage (V)
6.58
6.64
brightness (cd/m2)
3023
2714
electrical power efficiency (lm/W)
59.0
51.1
external quantum efficiency (%)
55.6
48
chromaticity (x, y)
(0.413, 0.400)
(0.412, 0.399)
R9
4.8
1.9
Ra
79.5
78.9
Ito, Norihiro, Anjiki, Takashi
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